US12583937B2ActiveUtilityA1

Compositions and methods for the diagnosis and treatment of tumor

82
Assignee: GENENTECH INCPriority: Nov 30, 2009Filed: Mar 16, 2022Granted: Mar 24, 2026
Est. expiryNov 30, 2029(~3.4 yrs left)· nominal 20-yr term from priority
A61K 47/6813A61K 47/6849A61K 47/6809A61K 47/6817A61K 47/6869A61K 47/6857A61K 47/6851C07K 2317/92C07K 16/3069C07K 16/3023A61K 2039/505A61K 31/537C07K 2317/76C07K 2317/56C07K 2317/14C07K 16/18A61K 45/06G01N 33/57545G01N 33/5759G01N 33/5752A61K 47/68033A61K 47/68031C07K 2317/77C07K 2317/73C07K 2317/567C07K 2317/565C07K 2317/24C07K 16/28A61P 37/04A61P 35/00C07K 16/30G01N 33/57492G01N 33/57449G01N 33/57423
82
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Claims

Abstract

The present invention is directed to compositions of matter useful for the diagnosis and treatment of tumor in mammals and to methods of using those compositions of matter for the same.

Claims

exact text as granted — not AI-modified
What is claimed is: 
     
         1 . A method of inhibiting the growth of a cell that expresses a TAT211 polypeptide comprising the amino acid sequence of SEQ ID NO:2 or an extracellular domain thereof, said method comprising contacting said cell with an antibody comprising:
 (a) a CDR-L1 sequence of SEQ ID NO: 21;   (b) a CDR-L2 sequence of SEQ ID NO: 35;   (c) a CDR-L3 sequence of SEQ ID NO: 39;   (d) a CDR-H1 sequence of SEQ ID NO: 42;   (e) a CDR-H2 sequence of SEQ ID NO: 46; and   (f) a CDR-H3 sequence of SEQ ID NO: 61;   wherein the binding of said antibody to said TAT211 polypeptide causes an inhibition of growth of said cell.   
     
     
         2 . The method of  claim 1 , wherein said cell is an ovarian cancer cell. 
     
     
         3 . The method of  claim 1 , wherein said cell is a lung cancer cell. 
     
     
         4 . A method of therapeutically treating a mammal having a cancerous tumor comprising cells that express a TAT211 polypeptide comprising the amino acid sequence of SEQ ID NO:2 or an extracellular domain thereof, said method comprising administering to said mammal a therapeutically effective amount of an antibody comprising:
 (a) a CDR-L1 sequence of SEQ ID NO: 21;   (b) a CDR-L2 sequence of SEQ ID NO: 35;   (c) a CDR-L3 sequence of SEQ ID NO: 39;   (d) a CDR-H1 sequence of SEQ ID NO: 42;   (e) a CDR-H2 sequence of SEQ ID NO: 46; and   (f) a CDR-H3 sequence of SEQ ID NO: 61;   thereby effectively treating said mammal.   
     
     
         5 . The method of  claim 4 , wherein said cells are ovarian cancer cells. 
     
     
         6 . The method of  claim 4 , wherein said cells are lung cancer cells.

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